Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_assertion description "[It has become apparent that there are very few highly recurrently mutated genes such as TP53, PIK3CA, and GATA3, that no two breast cancers display an identical repertoire of somatic genetic alterations at base-pair resolution and that there might not be a single highly recurrently mutated gene that defines each of the intrinsic subtypes of breast cancer (ie, basal-like, HER2-enriched, luminal A, and luminal B).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_assertion evidence source_evidence_literature NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_assertion SIO_000772 25713166 NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_assertion wasDerivedFrom befree-2016 NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_assertion wasGeneratedBy ECO_0000203 NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266174.RAA-9sog1NaAh6ZqGgBjibWp5BDD4XcG_8ODMcNmBPDfA130_provenance.